Vestergaard-Bogind B, Bennekou P
Biochim Biophys Acta. 1982 May 21;688(1):37-44. doi: 10.1016/0005-2736(82)90576-4.
The time-dependence of ionophore A23187-induced changes in the conductance of the Ca2+-sensitive K+ channels of the human red cell has been monitored with ion-specific electrodes. The membrane potential was reflected in CCCP-mediated pH changes in a buffer-free extracellular medium, and changes in extracellular K+ activity and electrode potential of an extracellular Ca2+-electrode were recorded. Within a narrow range of ionophore-mediated Ca2+ influx, the above-mentioned parameters were found to oscillate when ionophore was added to a suspension of glucose-fed cells. The period of oscillation was about 2 min/cycle depending on ionophore concentration, and the amplitude of hyperpolarization was about 60 mV, corresponding to a maximal gK+ of the same magnitude as gCl-. Without CCCP present no oscillation in K+ conductance was observed. The Ca2+ affinity for the opening process was in the micromolar range. The closing of the K+ channels was a spontaneous process in that the depolarization was well under way before the Ca2+-ATPase-mediated Ca2+ net efflux started. Below the Ca2+ influx range for oscillations, no response was observed for up to 20 min after the addition of ionophore. Above the upper limit, a permanent hyperpolarization resulted with an extracellular K+ activity increasing monotonically as a function of time. In experiments with ATP-depleted cells, responses of the latter type ensued at all ionophore concentrations above the lower limit. Addition of surplus EGTA to suspensions of hyperpolarized cells restores the normal membrane potential in the case of glucose-fed cells, whereas the K+-channels in ATP-depleted cells remained open.
已使用离子特异性电极监测了离子载体A23187诱导的人红细胞Ca2+敏感性K+通道电导变化的时间依赖性。在无缓冲的细胞外介质中,膜电位通过CCCP介导的pH变化反映出来,并记录细胞外K+活性和细胞外Ca2+电极的电极电位变化。在离子载体介导的Ca2+流入的狭窄范围内,当向葡萄糖喂养的细胞悬液中加入离子载体时,发现上述参数会发生振荡。振荡周期约为2分钟/循环,具体取决于离子载体浓度,超极化幅度约为60 mV,对应于与gCl-大小相同的最大gK+。不存在CCCP时,未观察到K+电导的振荡。Ca2+对开放过程的亲和力在微摩尔范围内。K+通道的关闭是一个自发过程,因为在Ca2+ - ATP酶介导的Ca2+净流出开始之前,去极化就已经充分进行。在振荡的Ca2+流入范围以下,加入离子载体后长达20分钟未观察到反应。在高于上限时,会导致永久性超极化,细胞外K+活性随时间单调增加。在对ATP耗尽细胞进行的实验中,在所有高于下限的离子载体浓度下都会出现后一种类型的反应。向超极化细胞悬液中添加过量的EGTA,对于葡萄糖喂养的细胞可恢复正常膜电位,而ATP耗尽细胞中的K+通道仍保持开放。